Comparative analysis of mesenchymal stem cells from bone marrow, cartilage, and adipose tissue

被引:269
作者
Peng, Linyi [1 ,3 ]
Jia, Zhuqing [1 ]
Yin, Xinhua [3 ]
Zhang, Xin [2 ]
Liu, Yinan [1 ]
Chen, Ping [1 ]
Ma, Kangtao [1 ]
Zhou, Chunyan [1 ]
机构
[1] Peking Univ, Hlth Sci Ctr, Sch Basic Med Sci, Dept Biochem & Mol Biol, Beijing 100083, Peoples R China
[2] Peking Univ, Hlth Sci Ctr, Inst Sport Med, Beijing 100083, Peoples R China
[3] Harbin Med Univ, Hosp Affiliated 2, Dept Cardiol, Harbin, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
D O I
10.1089/scd.2007.0217
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem cells (MSCs) isolated from bone marrow (BM), cartilage, and adipose tissue (AT) possess the capacity for self-renewal and the potential for multilineage differentiation, and are therefore perceived as attractive sources of stem cells for cell therapy. However, MSCs from these different sources have different characteristics. We compared MSCs of adult Sprague Dawley rats derived from these three sources in terms of their immunophenotypic characterization, proliferation capacity, differentiation ability, expression of angiogenic cytokines, and anti-apoptotic ability. According to growth curve, cell cycle, and telomerase activity analyses, MSCs derived from adipose tissue (AT-MSCs) possess the highest proliferation potential, followed by MSCs derived from BM and cartilage (BM-MSCs and C-MSCs). In terms of multilineage differentiation, MSCs from all three sources displayed osteogenic, adipogenic, and chondrogenic differentiation potential. The result of real-time RT-PCR indicated that these cells all expressed angiogenic cytokines, with some differences in expression level. Flow cytometry and MTT analysis showed that C-MSCs possess the highest resistance toward hydrogen peroxide-induced apoptosis, while AT-MSCs exhibited high tolerance to serum deprivation-induced apoptosis. Both AT and cartilage are attractive alternatives to BM as sources for isolating MSCs, but these differences must be considered when choosing a stem cell source for clinical application.
引用
收藏
页码:761 / 773
页数:13
相关论文
共 27 条
[1]   Human mesenchymal stem cells modulate allogeneic immune cell responses [J].
Aggarwal, S ;
Pittenger, MF .
BLOOD, 2005, 105 (04) :1815-1822
[2]   Therapeutic angiogenesis using autologous bone marrow stromal cells: Improved blood flow in a chronic limb ischemia model [J].
Al-Khaldi, A ;
Al-Sabti, H ;
Galipeau, J ;
Lachapelle, K .
ANNALS OF THORACIC SURGERY, 2003, 75 (01) :204-209
[3]   Plasticity of clonal populations of dedifferentiated adult human articular chondrocytes [J].
Barbero, A ;
Ploegert, S ;
Heberer, M ;
Martin, I .
ARTHRITIS AND RHEUMATISM, 2003, 48 (05) :1315-1325
[4]   Human adipose tissue-derived stem cells differentiate into endothelial cells in vitro and improve postnatal neovascularization in vivo [J].
Cao, Y ;
Sun, Z ;
Liao, LM ;
Meng, Y ;
Han, Q ;
Zhao, RCH .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 332 (02) :370-379
[5]   Bone marrow stromal cells generate muscle cells and repair muscle degeneration [J].
Dezawa, M ;
Ishikawa, H ;
Itokazu, Y ;
Yoshihara, T ;
Hoshino, M ;
Takeda, S ;
Ide, C ;
Nabeshima, Y .
SCIENCE, 2005, 309 (5732) :314-317
[6]   A comparative assessment of cartilage and joint fat pad as a potential source of cells for autologous therapy development in knee osteoarthritis [J].
English, A. ;
Jones, E. A. ;
Corscadden, D. ;
Henshaw, K. ;
Chapman, T. ;
Emery, P. ;
McGonagle, D. .
RHEUMATOLOGY, 2007, 46 (11) :1676-1683
[7]   Cardioprotective c-kit+ cells are from the bone marrow and regulate the myocardial balance of angiogenic cytokines [J].
Fazel, Shafie ;
Cimini, Massimo ;
Chen, Liwen ;
Li, Shuhong ;
Angoulvant, Denis ;
Fedak, Paul ;
Verma, Subodh ;
Weisel, Richard D. ;
Keating, Armand ;
Li, Ren-Ke .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (07) :1865-1877
[8]   Therapeutic angiogenesis for ischemic cardiovascular disease [J].
Freedman, SB ;
Isner, JM .
JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 2001, 33 (03) :379-393
[9]   Isolated allogeneic bone marrow-derived mesenchymal cells engraft and stimulate growth in children with osteogenesis imperfecta: Implications for cell therapy of bone [J].
Horwitz, EM ;
Gordon, PL ;
Koo, WKK ;
Marx, JC ;
Neel, MD ;
McNall, RY ;
Muul, L ;
Hofmann, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (13) :8932-8937
[10]   Comparative analysis of mesenchymal stem cells from bone marrow, umbilical cord blood, or adipose tissue [J].
Kern, Susanne ;
Eichler, Hermann ;
Stoeve, Johannes ;
Klueter, Harald ;
Bieback, Karen .
STEM CELLS, 2006, 24 (05) :1294-1301